Diehl G E, Grevers G, Kastenbauer E
Klinik und Poliklinik für Hals-Nasen-Ohren-Kranke der Ludwig-Maximilians-Universität München.
Laryngorhinootologie. 1990 Sep;69(9):454-9. doi: 10.1055/s-2007-998229.
There is an increased risk of malignancy in patients with genetically determined or acquired immunosuppression. The authors report a case of a 70-year-old patient with a lymphoplasmocytic immunocytoma who developed 19 squamous-cell carcinomas (SCC) and nine basal-cell carcinomas (BCC) over a three-year period. This was the reason to review 100 cases of malignant lymphomas for evidence of additional malignancies. Of these patients, 15% had one or more SCC or BCC in the head and neck area. The age range was 59 to 79 years (mean, 71.7 years) and the male:female ratio 11:4. One or more SCC arose in 93% of these patients, 36% developed an additional one or more BCC, and BCC alone occurred in 7%. The usual ratio of BCC:SCC is 10:1; in the authors' patients, by contrast, this ratio was 6:14. In 12 cases, SCC and BCC were located on the skin. The remaining cases of SCC developed in the oral mucosa, the tonsils and the hypopharynx. In 13 cases, low-grade malignant lymphomas were found and in two cases high-grade malignant lymphomas were found. The SCC were clinically aggressive. Thirty-six percent of the patients had recurrent lesions, 43% multiple neoplasms, and 50% metastases. Histologically, the SCC showed moderate to poor differentiation, a high degree of cell polymorphism and mitotic activity, and deep tissue infiltration. There are several explanations for the increased incidence of neoplasms in patients with immunodeficiency disorders. The surveillance function of the immune system may be impaired due to the disease itself or due to the treatment for immunosuppression. Immunosuppressive and cytotoxic agents are potential carcinogens.(ABSTRACT TRUNCATED AT 250 WORDS)
对于具有遗传决定的或后天获得性免疫抑制的患者,发生恶性肿瘤的风险会增加。作者报告了一例70岁患有淋巴浆细胞免疫细胞瘤的患者,该患者在三年时间里发展出19例鳞状细胞癌(SCC)和9例基底细胞癌(BCC)。这就是回顾100例恶性淋巴瘤病例以寻找其他恶性肿瘤证据的原因。在这些患者中,15%在头颈部区域有一个或多个SCC或BCC。年龄范围为59至79岁(平均71.7岁),男女比例为11:4。这些患者中有93%出现一个或多个SCC,36%又发展出一个或多个BCC,仅发生BCC的占7%。BCC与SCC的通常比例为10:1;相比之下,作者的患者中该比例为6:14。12例中,SCC和BCC位于皮肤上。其余SCC病例发生在口腔黏膜、扁桃体和下咽。13例中发现低度恶性淋巴瘤,2例中发现高度恶性淋巴瘤。SCC在临床上具有侵袭性。36%的患者有复发病变,43%有多发性肿瘤,50%有转移。组织学上,SCC显示中度至低度分化、高度细胞多形性和有丝分裂活性,以及深部组织浸润。免疫缺陷疾病患者肿瘤发病率增加有多种解释。免疫系统的监测功能可能因疾病本身或免疫抑制治疗而受损。免疫抑制剂和细胞毒性药物是潜在的致癌物。(摘要截短于250字)